Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K951683 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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AVI Sterile Impad Rigid Sole Foot Cover, Left Foot Product Code:6067 | 2 | 10/01/2010 | Covidien LP |
AVI Sterile Impad Rigid Sole Foot Cover, Right Foot Product Code:6066 | 2 | 10/01/2010 | Covidien LP |
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